This paper presents an integrated theoretical framework bridging macroscopic tensegrity mechanics with microscopic mechanotransduction pathways governed by the Piezo1/2 ion channels. While conventional biophysical paradigms often focus on static mechanical loading or pharmacological blockade to mitigate myofascial hypertonicity, the Axis 0 framework introduces a purely kinetic alternative. By utilizing periodic, mirror-symmetric oscillations propagated along continuous kinetic chains, the myofascial matrix actively triggers a synchronized functional opening of deep-tissue Piezo channels. This dynamic process induces immediate fluid pressure redistribution within the non-Newtonian extracellular matrix, driving the mechanosensitive sensors into a state of dynamic desensitization (saturation). Concurrently, this global equalization of mechanical tension halts intracellular calcium-mediated alarm signaling, promotes the nuclear translocation reversal of Yes-associated protein (YAP), and initiates a thixotropic gel-to-sol transition within the fascial network. Consequently, local tissue stiffness collapses toward a mechanical zero-point, achieving a state of "Mechanical Transparency" that can be quantitatively validated via structural feedback analysis and shear wave elastography. This model establishes a non-invasive, kinematically calibrated methodology that harmonizes structural re-engineering with native human physiological principles. Keywords: Piezo1/2 Channels; Mechanotransduction; Biotensegrity; Dynamic Desensitization; Mechanical Transparency; Myofascial Network; Thixotropy; YAP Nuclear Translocation; Isotropic Tension; Kinetic Chains; Mechanical Zero-Point.